510(k) K970194 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
PROFORM CEMENTED TITANIUM REVISION FEMORAL COMPONENT
| Applicant | Stelkast Company, Pittsburgh PA, US |
| Decision | Substantially Equivalent, Apr 14, 1997 |
| Received | Jan 21, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970194
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.